Publication: Acute myocardial infarction, ischemic cerebrovascular disease and variceal bleeding due to portal vein thrombosis in a patient with hereditary thrombophilia
dc.contributor.buuauthor | Baran, Bülent | |
dc.contributor.buuauthor | Yılmaz, Yusuf | |
dc.contributor.buuauthor | Algın, Oktay | |
dc.contributor.buuauthor | Keskin, Murat | |
dc.contributor.buuauthor | Kıyıcı, Murat | |
dc.contributor.buuauthor | Kocamaz, Güzin | |
dc.contributor.buuauthor | Dolar, Enver | |
dc.contributor.department | Tıp Fakültesi | |
dc.contributor.department | Tıp Fakültesi | |
dc.contributor.department | Tıp Fakültesi | |
dc.contributor.department | Radyoloji Ana Bilim Dalı | |
dc.contributor.department | İç Hastalıkları Ana Bilim Dalı | |
dc.contributor.department | Gastroenteroloji Ana Bilim Dalı | |
dc.contributor.orcid | 0000-0003-4518-5283 | |
dc.contributor.orcid | 0000-0001-7966-2346 | |
dc.contributor.orcid | 0000-0002-3208-6211 | |
dc.contributor.orcid | 0000-0002-3877-8366 | |
dc.contributor.orcid | 0000-0003-4526-4352 | |
dc.contributor.researcherid | K-6651-2012 | |
dc.contributor.researcherid | AAG-9177-2021 | |
dc.contributor.researcherid | A-7978-2012 | |
dc.contributor.scopusid | 35955740500 | |
dc.contributor.scopusid | 22936014300 | |
dc.contributor.scopusid | 23995109100 | |
dc.contributor.scopusid | 23050640000 | |
dc.contributor.scopusid | 6507627491 | |
dc.contributor.scopusid | 23995302100 | |
dc.contributor.scopusid | 6602075084 | |
dc.date.accessioned | 2024-02-27T07:38:18Z | |
dc.date.available | 2024-02-27T07:38:18Z | |
dc.date.issued | 2008-04 | |
dc.description.abstract | We report On a 43-year-old female patient with multiple thrombotic risk factors who, in a few months, developed acute myocardial infarction, an ischemic cerebrovascular event and variceal bleeding due to portal vein thrombosis. The factor V Leiden mutation was carried in heterozygous form, homocysteine was elevated at 19.6 mu mol/l, and methylene-tetrahydrofolate reductase C677T mutation was carried in. homozygous form. Moderately increased plasma homocysteine level and a reduced protein S activity were evident. Anticardiolipin IgG antibodies were mildly positive. We conclude that the presence of multiple genetic and environmental risk factors greatly amplifies the risk of clinical thrombotic events. | |
dc.identifier.citation | Baran, B. vd. (2008). "Acute myocardial infarction, ischemic cerebrovascular disease and variceal bleeding due to portal vein thrombosis in a patient with hereditary thromblophilia". Blood Coagulation and Fibrinolysis, 19(3), 243-246. | |
dc.identifier.endpage | 246 | |
dc.identifier.issn | 0957-5235 | |
dc.identifier.issn | 1473-5733 | |
dc.identifier.issue | 3 | |
dc.identifier.pubmed | 18388507 | |
dc.identifier.scopus | 2-s2.0-41849132863 | |
dc.identifier.startpage | 243 | |
dc.identifier.uri | https://doi.org/10.1097/MBC.0b013e3282f30ae5 | |
dc.identifier.uri | https://journals.lww.com/bloodcoagulation/Fulltext/2008/04000/Acute_myocardial_infarction,_ischemic.12.aspx | |
dc.identifier.uri | https://hdl.handle.net/11452/39989 | |
dc.identifier.volume | 19 | |
dc.identifier.wos | 000255228300012 | |
dc.indexed.scopus | Scopus | |
dc.indexed.wos | SCIE | |
dc.language.iso | en | |
dc.publisher | Lippincott Williams & Wilkins | |
dc.relation.journal | Blood Coagulation and Fibrinolysis | |
dc.relation.publicationcategory | Makale - Uluslararası Hakemli Dergi | |
dc.rights | info:eu-repo/semantics/closedAccess | |
dc.subject | Factor V Leiden mutation | |
dc.subject | Hereditary thrombophilia | |
dc.subject | Methylenetetrahydrofolate mutation | |
dc.subject | Portal vein thrombosis | |
dc.subject | Factor-v-leiden | |
dc.subject | Venous thrombosi | |
dc.subject | Antiphospholipid antibodies | |
dc.subject | Cirrhotic-patients | |
dc.subject | Risk | |
dc.subject | Metaanalysis | |
dc.subject | Disorders | |
dc.subject | Mutaion | |
dc.subject | Mthfr | |
dc.subject | Thromboembolism | |
dc.subject | Hematology | |
dc.subject.emtree | 5,10 methylenetetrahydrofolate reductase (FADH2) | |
dc.subject.emtree | Acetylsalicylic acid | |
dc.subject.emtree | Blood clotting factor 5 Leiden | |
dc.subject.emtree | Cardiolipin antibody | |
dc.subject.emtree | Carvedilol | |
dc.subject.emtree | Clopidogrel | |
dc.subject.emtree | Esomeprazole | |
dc.subject.emtree | Homocysteine | |
dc.subject.emtree | Immunoglobulin G antibody | |
dc.subject.emtree | Isosorbide mononitrate | |
dc.subject.emtree | Lansoprazole | |
dc.subject.emtree | Low molecular weight heparin | |
dc.subject.emtree | Nadroparin | |
dc.subject.emtree | Pravastatin | |
dc.subject.emtree | Protein S | |
dc.subject.emtree | Proton pump inhibitor | |
dc.subject.emtree | Acute heart infarction | |
dc.subject.emtree | Adult | |
dc.subject.emtree | Article | |
dc.subject.emtree | Bleeding | |
dc.subject.emtree | Case report | |
dc.subject.emtree | Cerebrovascular accident | |
dc.subject.emtree | Coronary stent | |
dc.subject.emtree | Drug substitution | |
dc.subject.emtree | Drug withdrawal | |
dc.subject.emtree | Environmental factor | |
dc.subject.emtree | Female | |
dc.subject.emtree | Gene mutation | |
dc.subject.emtree | Genetic risk | |
dc.subject.emtree | Heterozygosity | |
dc.subject.emtree | Homozygosity | |
dc.subject.emtree | Human | |
dc.subject.emtree | Percutaneous coronary intervention | |
dc.subject.emtree | Portal vein thrombosis | |
dc.subject.emtree | Portal vein thrombosis | |
dc.subject.emtree | Protein function | |
dc.subject.emtree | Risk factor | |
dc.subject.emtree | Thrombophilia | |
dc.subject.emtree | Thrombosis | |
dc.subject.emtree | Upper gastrointestinal bleeding | |
dc.subject.emtree | Varix bleeding | |
dc.subject.mesh | Adult | |
dc.subject.mesh | Factor V | |
dc.subject.mesh | Female | |
dc.subject.mesh | Genetic predisposition to disease | |
dc.subject.mesh | Humans | |
dc.subject.mesh | Methylenetetrahydrofolate reductase (nadph2) | |
dc.subject.mesh | Myocardial infarction | |
dc.subject.mesh | Portal vein | |
dc.subject.mesh | Stroke | |
dc.subject.mesh | Thrombophilia | |
dc.subject.mesh | Venous thrombosis | |
dc.subject.scopus | Mutation; Prothrombin; Activated Protein C Resistance | |
dc.subject.wos | Hematology | |
dc.title | Acute myocardial infarction, ischemic cerebrovascular disease and variceal bleeding due to portal vein thrombosis in a patient with hereditary thrombophilia | |
dc.type | Article | |
dc.wos.quartile | Q4 | |
dspace.entity.type | Publication | |
local.contributor.department | Tıp Fakültesi/İç Hastalıkları Ana Bilim Dalı | |
local.contributor.department | Tıp Fakültesi/Radyoloji Ana Bilim Dalı | |
local.contributor.department | Tıp Fakültesi/Gastroenteroloji Ana Bilim Dalı | |
local.indexed.at | WOS | |
local.indexed.at | Scopus |
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